Last synced on 14 November 2025 at 11:06 pm

iFuse Implant System®

Page Type
Cleared 510(K)
510(k) Number
K190230
510(k) Type
Traditional
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2019
Days to Decision
56 days
Submission Type
Summary

iFuse Implant System®

Page Type
Cleared 510(K)
510(k) Number
K190230
510(k) Type
Traditional
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2019
Days to Decision
56 days
Submission Type
Summary